Mechanism of formation of the contractile ring during cytokinesis
胞质分裂过程中收缩环的形成机制
基本信息
- 批准号:15207013
- 负责人:
- 金额:$ 31.62万
- 依托单位:
- 依托单位国家:日本
- 项目类别:Grant-in-Aid for Scientific Research (A)
- 财政年份:2003
- 资助国家:日本
- 起止时间:2003 至 2005
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
1)rho4 and rho5 genes of fission yeast was cloned. Rho4 regulates localization of F-actin patches and organization of microtubules, and thereby formation of cell wall and the septum. Localization of Rho4 is regulated by RhoGDI while activity of Rho4 is regulated by the RhoGAP Rga92)Sea urchin Cdc42 showed 87% homology to human Cdc42. It binds IQGAP and thus enhancesw actin polymerization. IQGAP localizes to the cleavage furrow during cytokinesis.3)It was established that the C-terminal 134 residues are necessary and sufficient for localization of Myo2 to the division site. This region contains Ser1444 which is phosphorylated during interphase but dephosphorylated during M-phase. This dephosphorylation enables Myo2 to target Mid1 which is transmitted from the nucleus to the equatorial cortex during G2.4)The Rho1GEFs Rgf1 and Rgf2 are localized to the growing ends of fission yeast cell during interphase, while to the septum region during mitosis and are involved in synthesis of cell wall … More and the septum. Rgf3 accumulates at the division site forming a ring during mitosis, and the ring contracts as cytokinesis progresses. Rgf3 is considered to control formation of both the contractile ring and the septum through activation of Rho1.5)We determined directionality of F-actins in the F-actin cables in fission yeast cells by decorating the F-actins using myosin S1. The barbed end of the F-actins in the interphase cables face the growing end of the cell during interphase. During mitosis, it reversed. We proposed a hypothesis that myosin V transports materials necessary for polarized growth of the cell to the cell ends during interphase, while transports those necessary for division to the division site during mitosis.6)Fission yeast actin-depolymerizing factor Adf1 is localized to the F-actin patches during interphase and to the contractile ring during mitosis and cytokinesis. Adf1 is involved in formation of the contractile ring through its F-actin-severing activity. Its binding to F-actin in the cell is competitive with the tropomyosin Cdc8. It was also found that Adf1 cooperates with myosin-II in formation of the contractile ring. We propose that Adf1 is necessary for formation and stability of the contractile ring. Less
1)克隆了裂变酵母的rho4和rho5基因。Rho4调节f -肌动蛋白贴片的定位和微管的组织,从而调控细胞壁和隔膜的形成。Rho4的定位受RhoGDI调控,Rho4的活性受RhoGAP Rga92调控)海胆Cdc42与人Cdc42的同源性为87%。它结合IQGAP,从而增强肌动蛋白聚合。在细胞分裂过程中,IQGAP定位于卵裂沟。3) c端134残基是Myo2定位到分裂位点的必要和充分条件。该区域包含Ser1444,在间期磷酸化,但在m期去磷酸化。这种去磷酸化使Myo2能够靶向Mid1, Mid1在G2.4期间从细胞核传递到赤道皮层。Rho1GEFs Rgf1和Rgf2在间期时定位于分裂酵母细胞的生长端,而在有丝分裂时定位于隔膜区,参与细胞壁和隔膜的合成。在有丝分裂过程中,Rgf3聚集在分裂部位形成一个环,随着细胞质分裂的进行,这个环收缩。Rgf3被认为通过激活rho1来控制收缩环和隔膜的形成。)我们通过使用肌球蛋白S1来修饰f -肌动蛋白,从而确定了裂变酵母细胞中f -肌动蛋白索中的f -肌动蛋白的方向性。间期时,间期索中f -肌动蛋白的倒刺端面向细胞的生长端。在有丝分裂期间,它反过来了。我们提出了一个假设,肌凝蛋白V在间期将细胞极化生长所需的物质运输到细胞末端,而在有丝分裂期间将分裂所需的物质运输到分裂部位。6)分裂酵母肌动蛋白解聚因子Adf1在间期定位于f -肌动蛋白斑块,在有丝分裂和细胞分裂时定位于收缩环。Adf1通过切断f -actin活性参与了收缩环的形成。它在细胞中与f -肌动蛋白的结合与原肌球蛋白Cdc8竞争。还发现Adf1与肌球蛋白- ii协同形成收缩环。我们认为Adf1对于收缩环的形成和稳定是必要的。少
项目成果
期刊论文数量(50)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Myosin-II reorganization during mitosis is controlled temporally by its dephosphorylation and spatially by Mid1 in fission yeast.
- DOI:10.1083/jcb.200402097
- 发表时间:2004-06-07
- 期刊:
- 影响因子:0
- 作者:Motegi F;Mishra M;Balasubramanian MK;Mabuchi I
- 通讯作者:Mabuchi I
A novel actin-bunding kinesin-related protein from Dictyostelium discoideum.
一种来自盘基网柄菌的新型肌动蛋白结合驱动蛋白相关蛋白。
- DOI:
- 发表时间:2004
- 期刊:
- 影响因子:0
- 作者:Iwai;S.
- 通讯作者:S.
Rho1-GEFs Rgf1 and Rgf2 are involved in formation of cell wall and septum, while Rgf3 is involved in cytokinesis in fission yeast
- DOI:10.1111/j.1365-2443.2005.00908.x
- 发表时间:2005-12-01
- 期刊:
- 影响因子:2.1
- 作者:Mutoh, T;Nakano, K;Mabuchi, I
- 通讯作者:Mabuchi, I
Kentaro Nakano: "The small GTPase Rho4 is involved in controlling cell morphology and septation in fission yeast."Genes to Cells. 8. 357-370 (2003)
Kentaro Nakano:“小型 GTP 酶 Rho4 参与控制裂殖酵母的细胞形态和分隔。”《基因到细胞》。
- DOI:
- 发表时间:
- 期刊:
- 影响因子:0
- 作者:
- 通讯作者:
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MABUCHI Issei其他文献
MABUCHI Issei的其他文献
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{{ truncateString('MABUCHI Issei', 18)}}的其他基金
Structure, formation, and contraction of the contractile ring
收缩环的结构、形成和收缩
- 批准号:
22247031 - 财政年份:2010
- 资助金额:
$ 31.62万 - 项目类别:
Grant-in-Aid for Scientific Research (A)
Molecular mechanism that induces cytokinesis
诱导胞质分裂的分子机制
- 批准号:
19370080 - 财政年份:2007
- 资助金额:
$ 31.62万 - 项目类别:
Grant-in-Aid for Scientific Research (B)
Mechanism of contractile ring formation during cytokinesis
胞质分裂过程中收缩环形成的机制
- 批准号:
12490008 - 财政年份:2000
- 资助金额:
$ 31.62万 - 项目类别:
Grant-in-Aid for Scientific Research (B)
Mechanisms of formation and destruction of the contractile ring during cytokinesis
胞质分裂过程中收缩环的形成和破坏机制
- 批准号:
10213101 - 财政年份:1998
- 资助金额:
$ 31.62万 - 项目类别:
Grant-in-Aid for Scientific Research on Priority Areas
Molecular mechanism of cytokinesis in animal cells
动物细胞胞质分裂的分子机制
- 批准号:
06404004 - 财政年份:1994
- 资助金额:
$ 31.62万 - 项目类别:
Grant-in-Aid for Scientific Research (A)
STUDIES ON DYNAMIC PROPERITIES OF CYTOSKELETAL FILAMENT SYSTEMS
细胞骨架丝系统的动力学特性研究
- 批准号:
04304057 - 财政年份:1992
- 资助金额:
$ 31.62万 - 项目类别:
Grant-in-Aid for Co-operative Research (A)
Molecular mechanism of cytokinesis
胞质分裂的分子机制
- 批准号:
02455009 - 财政年份:1990
- 资助金额:
$ 31.62万 - 项目类别:
Grant-in-Aid for General Scientific Research (B)
Role of microtubules and related proteins on cellular function
微管和相关蛋白质对细胞功能的作用
- 批准号:
60300007 - 财政年份:1985
- 资助金额:
$ 31.62万 - 项目类别:
Grant-in-Aid for Co-operative Research (A)
Molecular mechanism of cutokinesis
细胞运动的分子机制
- 批准号:
59490013 - 财政年份:1984
- 资助金额:
$ 31.62万 - 项目类别:
Grant-in-Aid for General Scientific Research (B)
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